Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_assertion description "[BMP4 deletions were detected in two patients: a patient affected with SHORT syndrome and a patient with anterior segment anomalies along with craniofacial dysmorphism and cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_assertion evidence source_evidence_literature NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_assertion SIO_000772 21340693 NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_assertion wasDerivedFrom befree-20140225 NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_assertion wasGeneratedBy ECO_0000203 NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP526734.RADfGz1RYR1GZivHlDdSE5plnAYW1xih132DznW8Y4F_U130_provenance.